MEDLIB
Orphanet Database

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Болезней
4 552Генов
8 700Фенотипов

Mucopolysaccharidosis type 2, attenuated form

ORPHA:217093Клин. подтип
X-linked recessive

Mucopolysaccharidosis type 2, severe form

ORPHA:217085Клин. подтип
X-linked recessive

Mucopolysaccharidosis type 3

ORPHA:581Заболевание
Autosomal recessive

Mucopolysaccharidosis type 4

ORPHA:582Заболевание
Autosomal recessive

Mucopolysaccharidosis type 4A

ORPHA:309297Клин. подтип
Autosomal recessive

Mucopolysaccharidosis type 4B

ORPHA:309310Клин. подтип
Autosomal recessive

Mucopolysaccharidosis type 6

ORPHA:583Заболевание
Autosomal recessive

Mucopolysaccharidosis type 6, rapidly progressing

ORPHA:276212Клин. подтип
Autosomal recessive

Mucopolysaccharidosis type 6, slowly progressing

ORPHA:276223Клин. подтип
Autosomal recessive

Mucopolysaccharidosis type 7

ORPHA:584Заболевание
Autosomal recessive

Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders

ORPHA:505248Мальформация
Autosomal recessive

Mucous membrane pemphigoid

ORPHA:46486Заболевание
Not applicable

Mueller-Weiss syndrome

ORPHA:566943Заболевание

Muenke syndrome

ORPHA:53271Мальформация
Autosomal dominant

Mulibrey nanism

ORPHA:2576Мальформация
Autosomal recessive

Multicentric carpo-tarsal osteolysis with or without nephropathy

ORPHA:2774Мальформация
Autosomal dominant

Multicentric osteolysis-nodulosis-arthropathy spectrum

ORPHA:371428Заболевание
Autosomal recessive

Multicentric reticulohistiocytosis

ORPHA:139436Заболевание
Not applicable

Multicystic dysplastic kidney

ORPHA:1851Морф. аномалия
Not applicable

Multifocal atrial tachycardia

ORPHA:3282Заболевание
Not applicable

Multifocal infantile hemangioma with extracutenous involvement

ORPHA:2123Заболевание
Not applicable

Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome

ORPHA:464321Заболевание
Not applicable

Multifocal motor neuropathy

ORPHA:641Заболевание
Unknown

Multifocal pattern dystrophy simulating fundus flavimaculatus

ORPHA:99003Заболевание
Autosomal dominant